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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428834Generated: October 26, 2026

Thiophenol → 1-Nitro-3-(phenylsulfanyl)benzene

https://huagongshe.com/reaction/1428834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Iodo-3-nitrobenzeneHCID 12574—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
Product1-Nitro-3-(phenylsulfanyl)benzeneHCID 142232—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of thiophenol (1.0 g, 9.1 mmol), 3-iodonitrobenzene (1.9 g, 7.6 mmol), CuI (0.14 g, 0.76 mmol), K2CO3 (1.67 g, 12.1 mmol), and DMF (10 mL) was heated to 100° C. in a flame-dried sealed tube for 16 h. The mixture was allowed to cool and was poured over ice. The resulting mixture was extracted with EtOAc (2×), and the organic extracts were combined and washed sequentially with equal volumes of aqueous 1M HCl, water, and aqueous 1M NaOH. The solution was dried, concentrated, and the residue was purified by FCC (100:0 to 95:5 hexanes/EtOAc) to provide the titled compound, which was contaminated with ca. 10% thiophenol (1.43 g), and was taken on to subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937078B2
Source datasetuspto-grants-2015_01
ORD IDord-0bcc46a1b38348919cfa06ce86502a56
Source noteuspto-grants-2015_01